FDA 510(k) Application Details - K222124

Device Classification Name	Needle, Hypodermic, Single Lumen   More FDA Info for this Device
510(K) Number	K222124
Device Name	Needle, Hypodermic, Single Lumen
Applicant	Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd No. 2 Guanyin Road, Economic Development Zone, Taihu Anqing City 246400 CN Other 510(k) Applications for this Company
Contact	Bingyi Xiang Other 510(k) Applications for this Contact
Regulation Number	880.5570   More FDA Info for this Regulation Number
Classification Product Code	FMI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/18/2022
Decision Date	11/04/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review